Rabia Faridi

708 total citations
13 papers, 353 citations indexed

About

Rabia Faridi is a scholar working on Molecular Biology, Sensory Systems and Plant Science. According to data from OpenAlex, Rabia Faridi has authored 13 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Sensory Systems and 3 papers in Plant Science. Recurrent topics in Rabia Faridi's work include Hearing, Cochlea, Tinnitus, Genetics (5 papers), RNA regulation and disease (5 papers) and Mitochondrial Function and Pathology (3 papers). Rabia Faridi is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (5 papers), RNA regulation and disease (5 papers) and Mitochondrial Function and Pathology (3 papers). Rabia Faridi collaborates with scholars based in Pakistan, United States and United Kingdom. Rabia Faridi's co-authors include Muhammad Idrees, Thomas B. Friedman, Sheikh Riazuddin, Asma Ali Khan, Atteeq U. Rehman, Saima Riazuddin, Suzanne M. Leal, Robert J. Morell, Michael Hoa and William G. Newman and has published in prestigious journals such as Human Mutation, Human Genetics and European Journal of Human Genetics.

In The Last Decade

Rabia Faridi

13 papers receiving 348 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Rabia Faridi Pakistan	10	181	96	81	44	42	13	353
Mostafa Kandil Morocco	11	129 0.7×	95 1.0×	36 0.4×	50 1.1×	148 3.5×	28	400
Andreas Th. Müller Austria	9	126 0.7×	91 0.9×	23 0.3×	38 0.9×	56 1.3×	30	290
Valerie E. Vancollie United Kingdom	8	162 0.9×	53 0.6×	17 0.2×	17 0.4×	60 1.4×	12	278
Kathryn Hall United States	10	175 1.0×	66 0.7×	19 0.2×	10 0.2×	108 2.6×	21	340
Mitsuyoshi Nagura Japan	6	126 0.7×	116 1.2×	44 0.5×	66 1.5×	7 0.2×	11	381
Qian Pan China	10	298 1.6×	9 0.1×	34 0.4×	32 0.7×	86 2.0×	56	485
Arjan Pm de Brouwer Netherlands	6	94 0.5×	30 0.3×	15 0.2×	16 0.4×	60 1.4×	14	209
Regie Lyn P. Santos‐Cortez United States	9	150 0.8×	110 1.1×	9 0.1×	40 0.9×	30 0.7×	31	278
Hitoshi Sasajima Japan	10	230 1.3×	42 0.4×	67 0.8×	9 0.2×	24 0.6×	15	388
Pei‐Hsuan Wu Taiwan	7	136 0.8×	9 0.1×	28 0.3×	10 0.2×	16 0.4×	17	242

Countries citing papers authored by Rabia Faridi

Since Specialization

Citations

This map shows the geographic impact of Rabia Faridi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Rabia Faridi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rabia Faridi more than expected).

Fields of papers citing papers by Rabia Faridi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rabia Faridi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Rabia Faridi. The network helps show where Rabia Faridi may publish in the future.

Co-authorship network of co-authors of Rabia Faridi

This figure shows the co-authorship network connecting the top 25 collaborators of Rabia Faridi. A scholar is included among the top collaborators of Rabia Faridi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Rabia Faridi. Rabia Faridi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Faridi, Rabia, Pamela Stratton, Noemi Salmeri, et al.. (2024). Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical Genetics. 105(5). 584–586. 4 indexed citations

Faridi, Rabia, Rizwan Yousaf, Sayaka Inagaki, et al.. (2024). Deafness DFNB128 Associated with a Recessive Variant of Human MAP3K1 Recapitulates Hearing Loss of Map3k1-Deficient Mice. Genes. 15(7). 845–845. 1 indexed citations

Faridi, Rabia, Cristina Fenollar‐Ferrer, Raymond T. O’Keefe, et al.. (2021). New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder. Human Genetics. 141(3-4). 805–819. 28 indexed citations

Faridi, Rabia, Parna Chattaraj, Rizwan Yousaf, et al.. (2021). Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria. European Journal of Human Genetics. 30(1). 42–52. 10 indexed citations

Faridi, Rabia, et al.. (2021). Genetic study of the resistance of faba bean (Vicia faba) against the fungus Ascochyta fabae through a genome‐wide association analysis. Plant Breeding. 140(3). 442–452. 9 indexed citations

Faridi, Rabia, Kelly King, Christopher Zalewski, et al.. (2020). Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome. Clinical Genetics. 99(2). 226–235. 24 indexed citations

Tona, Risa, Iván A. López, Cristina Fenollar‐Ferrer, et al.. (2020). Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness. Genes. 11(10). 1122–1122. 11 indexed citations

Faridi, Rabia, Risa Tona, Alessandra Brofferio, et al.. (2018). Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome. Human Mutation. 40(2). 162–176. 27 indexed citations

Rehman, Atteeq U., Jonathan E. Bird, Rabia Faridi, et al.. (2016). Mutational Spectrum ofMYO15Aand the Molecular Mechanisms of DFNB3 Human Deafness. Human Mutation. 37(10). 991–1003. 55 indexed citations

10.

Ali, Zulfiqar, et al.. (2016). FUNCTIONS OF PLANT’S BZIP TRANSCRIPTION FACTORS. The Pakistan Journal of Agricultural Sciences. 53(2). 303–314. 26 indexed citations

11.

Faridi, Rabia, Atteeq U. Rehman, Robert J. Morell, et al.. (2016). Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. Clinical Genetics. 91(2). 328–332. 35 indexed citations

12.

Faridi, Rabia, et al.. (2015). Gene Action Study for Morphological Traits in Sunflower (Helianthus annuus L.). American-Asian-Journal of agricultural & environmental sciences. 15(5). 769–775. 3 indexed citations

13.

Faridi, Rabia, et al.. (2011). Oncogenic potential of Human Papillomavirus (HPV) and its relation with cervical cancer. Virology Journal. 8(1). 269–269. 120 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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